IRB Coordinator: Regulatory Expert for Human Subjects

Mercy-Health-System-Corporation

Rockford (IL)

Hybrid

USD 54,000 - 84,000

Full time

5 days ago
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Benefits offered by this job

Medical
Dental
Vision
Life & Disability Insurance
FSA/HSA Options
Generous PTO

Job summary

Mercyhealth seeks an IRB Coordinator to provide regulatory expertise and administrative support for the Institutional Review Board overseeing human subject research. The role serves as the primary regulatory resource for investigators and staff, with a hybrid schedule and potential site visits to Mercyhealth locations.

The candidate will educate researchers, review applications for compliance, and prepare IRB documents.

Qualifications

  • Bachelor’s degree in biomedical, health science, social sciences or related field.
  • Knowledge of federal regulations and guidelines governing human subject research.
  • Experience in healthcare or human subject research preferred.
  • CIP and GCP certifications required or to be obtained per eligibility.

Responsibilities

  • Serve as subject-matter expert and guide researchers on human subject research design and conduct.
  • Review new research applications for compliance and required federally mandated elements.
  • Communicate items requiring clarification to Principal Investigators and prepare documentation.
  • Evaluate reports of unanticipated problems, noncompliance and continuing reviews.
  • Prepare agendas, meeting materials and minutes; maintain IRB files.

Skills

Regulatory knowledge
Attention to detail
Excellent written and verbal skills
Problem solving & critical thinking

Education

Bachelor's degree in biomedical/health sciences
CIP certification
GCP certification

Tools

Microsoft Office

Job description

Mercyhealth seeks an IRB Coordinator to provide regulatory expertise and administrative support for the Institutional Review Board overseeing human subject research. The role serves as the primary regulatory resource for investigators and staff, with a hybrid schedule and potential site visits to Mercyhealth locations.

The candidate will educate researchers, review applications for compliance, and prepare IRB documents.

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